NDC 51662-1514
Ondansetron 4 mg tablet, orally disintegrating
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-077.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA090469
- On the market since
- Mar 31, 2020
- Package NDCs
51662-1514-151662-1514-2- Official label
- DailyMed (National Library of Medicine), updated Jan 22, 2024
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